SCANLAN SUTURE-STATT— 510(k) K821887

Substantially Equivalent

Scanlan Intl., Inc.

FDA 510(k) clearance K821887 for SCANLAN SUTURE-STATT, Substantially Equivalent on 1982-07-28. Applicant: Scanlan Intl., Inc.. Device class: 1.

Clearance details

Applicant: Scanlan Intl., Inc.
Product code: Code HRQ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1982-06-25
Decision date: 1982-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K881937 — SURGICAL INSTRUMENTS1988-06-15

More clearances from Scanlan Intl., Inc.

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K911184 — SCANLAN/TAHERI VALVULOTOME1992-02-18
K864919 — SCANLAN (TM) VEIN/GRAFT HOLDER1987-01-12
K864920 — SCANLAN (TM) INSTRUMENT TRAY1987-01-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.